Canonical Allele Identifier: CA377378941
Community Standard Title: NM_033100.4(CDHR1):c.2041-1G>C
Gene: CDHR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.84214081G>C , CM000672.2:g.84214081G>C GRCh38
NC_000010.10:g.85973837G>C , CM000672.1:g.85973837G>C GRCh37
NC_000010.9:g.85963817G>C NCBI36
NG_028034.1:g.24426G>C

Transcript Alleles

HGVS Amino-acid Change
NM_033100.4:c.2041-1G>C MANE Select NP_149091.1:n.2041-1G>C
ENST00000623527.4:c.2041-1G>C MANE Select ENSP00000485478.1:n.2041-1G>C
NM_001171971.2:c.2040+733G>C NP_001165442.1:n.2040+733G>C
NM_001171971.3:c.2040+733G>C NP_001165442.1:n.2040+733G>C
NM_033100.3:c.2041-1G>C NP_149091.1:n.2041-1G>C
ENST00000332904.7:c.2040+733G>C ENSP00000331063.3:n.2040+733G>C
ENST00000372117.6:c.1256-1G>C
ENST00000459673.1:n.473-1G>C
ENST00000622973.1:c.659-1G>C
ENST00000623399.1:c.211+733G>C
ENST00000623527.3:c.2041-1G>C ENSP00000485478.1:n.2041-1G>C
XM_011540337.1:c.2215-1G>C XP_011538639.1:n.2215-1G>C
XM_011540338.1:c.2214+733G>C XP_011538640.1:n.2214+733G>C
XM_011540339.1:c.1594-1G>C XP_011538641.1:n.1594-1G>C